Hereditary pheochromocytoma-paraganglioma
MONDO:0017366Neoplasm predisposition characterized by an increased risk of paragangliomas (tumors that arise from neuroendocrine tissues distributed along the paravertebral axis from the base of the skull to the pelvis) and pheochromocytomas (paragangliomas that are confined to the adrenal medulla).
Also known as: familial pheochromocytoma-paraganglioma, hereditary paraganglioma-pheochromocytoma syndrome, hereditary pheochromocytoma-paraganglioma, SDHx-related paraganglioma-pheochromocytoma, hereditary paraganglioma-pheochromocytoma
1487 clinical trials for this condition and its sub-types, 6 tagged with Hereditary pheochromocytoma-paraganglioma itself.
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Browse by category →Sub-types of Hereditary pheochromocytoma-paraganglioma
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MAX-related tumor predisposition 0 trials
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TMEM127-related tumor predisposition 0 trials